There's a lot of confusion out there around genetic testing during pregnancy. Who should get tested? When? Is it a cause for concern, or a harmless preventative measure?
I wanted to clear up any confusion or misconceptions about genetic testing in today's episode of the podcast, so I invited Dr. Keisha Reddick back on the show to help me do so.
Dr. Reddick is a Maternal Fetal Medicine doctor and is up-to-date on everything you need to know about genetic testing and carrier testing for you and your baby.
We talk about the different kinds of genetic testing you may encounter, what trimester you can get them, and what each one will tell you. Dr. Reddick also talks about why she is such a proponent of genetic testing for high-risk pregnancies and anybody else who wants to be prepared with knowledge about their baby.
The vast majority of pregnancies are normal, but it's a good idea to prepare yourself mentally and ensure the safest delivery for your baby if there's any chance they might need extra care.
I also have a super-special offer for you on my Birth Preparation Course this December, and it won't be happening again anytime soon! Head to drnicolerankins.com/enroll and use the code DECEMBER, and you'll get $150 off the all-access level of the Birth Preparation Course.
In this Episode, You’ll Learn About:
Links Mentioned in the Episode
Nuchal Translucency - measures the thickness at the back of the baby’s neck by ultrasound
Requires specially trained ultrasound technician
NIPT (non invasive prenatal testing a.k.a. the gender test)
Blood test between 15-20 weeks Has largely been replaced by first trimester screening.
Chorionic Villus Sampling (CVS)
Diagnostic test that gives the most amount of information. Requires skilled practitioner. Not many doctors do this.
Diagnostic test that gives the most amount of information. Less risky than CVS. Requires skilled practitioner.